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Omni Laser KDT750

by Shanghai Omni Laser Skinology Co., Ltd.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06976855557508 UDI-DI Date1 Jan 2024ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Omni Laser
Generic Name
Intense pulsed light skin surface treatment system
Model / Reference
KDT750
Primary DI / UDI-DI
06976855557508
FDA Product Code
ONF
GMDN Term
Intense pulsed light skin surface treatment system
Device Class
Class II
Regulation Number
878.4810
GUDID distribution status
Not in Commercial Distribution

Other devices from Shanghai Omni Laser Skinology Co., Ltd.

Properties

  • Over-the-Counter
  • Manufacturing Date

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No